Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 1-Hexene | HCID 11597 | — |
| Reactant | 2-Amino-3-methylpyridine | HCID 15347 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Heptanophenone | HCID 74282 | — |
Reaction Steps
Under the same reaction procedure and conditions as in Example 1 (benzaldehyde 0.5 mmol, 2-amino-3-picoline 0.1 mmol, aniline 0.3 mmol, bezoic acid 0.03 mmol), 1-hexene and toluene at various amounts as shown in the following table 8, were added to each 500 ml pressure reactor. The mixture was stirred at normal temperature for 2-3 minutes and then combined with Rh(PPh3)3Cl 0.01 mmol. While the reactor was stopped with a stopper, the reactants were heated at 130 ° C. for 1 hour with stirring. After completion of the reaction, gas chromatography was conducted to determine the yields of heptanophenone, products according to 1-hexene and toluene of various amounts. The results are given in Table 8, below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06353139B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-e56a499df361484da4911e91fe4f2d06 |
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| Source note | uspto-grants-2002_03 |
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